Rhizomelic chondrodysplasia punctata (RCDP) is a group of disorders with overlapping clinical features including rhizomelia, chondrodysplasia punctata, coronal clefts, cervical dysplasia, congenital cataracts, profound postnatal growth retardation, severe intellectual disability, and seizures. Mutations in PEX7, GNPAT, and AGPS, all involved in the plasmalogen-biosynthesis pathway, have been described in individuals with RCDP. Here, we report the identification of mutations in another gene in plasmalogen biosynthesis, fatty acyl-CoA reductase 1 (FAR1), in two families affected by severe intellectual disability, early-onset epilepsy, microcephaly, congenital cataracts, growth retardation, and spasticity. Exome analyses revealed a homozygous ...
Rhizomelic chondrodysplasia punctata (RCDP) is a genetically heterogeneous, autosomal recessive diso...
Rhizomelic chondrodysplasia punctata (RCDP) is a genetically heterogeneous autosomal recessive syndr...
Background Rhizomelic chondrodysplasia punctata (RCDP) type 1 is among of the rare autosomal recessi...
Rhizomelic chondrodysplasia punctata (RCDP) is a group of disorders with overlapping clinical featur...
Investigators from Erlangen, Germany; Calgary, CA; and Kafranbel, Syria, identified muta...
Rhizomelic chondrodysplasia punctata (RCDP) is a heterogenous group of disorders due to defects in g...
Abstract The FAR1‐related phenotypes caused by the FAR1 gene encodes the peroxisomal protein fatty a...
PurposeIn this study we investigate the disease etiology in 12 patients with de novo variants in FAR...
Purpose: In this study we investigate the disease etiology in 12 patients with de novo variants in F...
To describe the neurologic profiles of Rhizomelic chondrodysplasia punctata (RCDP); a peroxisomal di...
We describe two brothers who presented at birth with bone growth abnormalities, followed by developm...
Rhizomelic chondrodysplasia punctata (RCDP) is a disorder of peroxisome metabolism result-ing from a...
Rhizomelic chondrodysplasia punctata (RCDP) is a genetic disorder which is clinically characterized ...
Key Clinical Message Rhizomelic chondrodysplasia punctata (RCDP) is a rare disorder (~1 in 100,000 l...
Very-long-chain fatty acids (VLCFAs) play important roles in membrane structure and cellular signali...
Rhizomelic chondrodysplasia punctata (RCDP) is a genetically heterogeneous, autosomal recessive diso...
Rhizomelic chondrodysplasia punctata (RCDP) is a genetically heterogeneous autosomal recessive syndr...
Background Rhizomelic chondrodysplasia punctata (RCDP) type 1 is among of the rare autosomal recessi...
Rhizomelic chondrodysplasia punctata (RCDP) is a group of disorders with overlapping clinical featur...
Investigators from Erlangen, Germany; Calgary, CA; and Kafranbel, Syria, identified muta...
Rhizomelic chondrodysplasia punctata (RCDP) is a heterogenous group of disorders due to defects in g...
Abstract The FAR1‐related phenotypes caused by the FAR1 gene encodes the peroxisomal protein fatty a...
PurposeIn this study we investigate the disease etiology in 12 patients with de novo variants in FAR...
Purpose: In this study we investigate the disease etiology in 12 patients with de novo variants in F...
To describe the neurologic profiles of Rhizomelic chondrodysplasia punctata (RCDP); a peroxisomal di...
We describe two brothers who presented at birth with bone growth abnormalities, followed by developm...
Rhizomelic chondrodysplasia punctata (RCDP) is a disorder of peroxisome metabolism result-ing from a...
Rhizomelic chondrodysplasia punctata (RCDP) is a genetic disorder which is clinically characterized ...
Key Clinical Message Rhizomelic chondrodysplasia punctata (RCDP) is a rare disorder (~1 in 100,000 l...
Very-long-chain fatty acids (VLCFAs) play important roles in membrane structure and cellular signali...
Rhizomelic chondrodysplasia punctata (RCDP) is a genetically heterogeneous, autosomal recessive diso...
Rhizomelic chondrodysplasia punctata (RCDP) is a genetically heterogeneous autosomal recessive syndr...
Background Rhizomelic chondrodysplasia punctata (RCDP) type 1 is among of the rare autosomal recessi...